首页> 外文期刊>Journal of Neuroscience Methods >Genotype identification of Math1/LacZ knockout mice based on real-time PCR with SYBR Green I dye.
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Genotype identification of Math1/LacZ knockout mice based on real-time PCR with SYBR Green I dye.

机译:基于实时PCR和SYBR Green I染料的Math1 / LacZ基因敲除小鼠的基因型鉴定。

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摘要

Knockout mice are widely used in all fields of biomedical research. Determining the genotype of every newborn mouse is a tedious task, usually performed by Southern blot hybridization or Polymerase Chain Reaction (PCR). We describe here a quick and simple genotype identification assay based on real-time PCR and SYBR((R)) Green I dye, without using fluorescent primers. The discrimination between the wild type and targeted alleles is based on a PCR design that leads to a different melting temperature for each product. The identification of the genotype is obvious immediately after amplification, and no post-PCR manipulations are needed, reducing cost and time. Therefore, while the real-time PCR amplification increases the sensitivity, the fact that the reactions tubes are never opened after amplification, reduces the risk of contamination and eliminates errors, which are common during the repeated handling of dozens of samples from the same mouse line. The protocol we provide was tested on Math1 knockoutmice, but is general, and may be utilized for any knockout line and real-time thermocycler, without any further modification, accessories or special reagents.
机译:敲除小鼠广泛用于生物医学研究的所有领域。确定每只新生小鼠的基因型是一项繁琐的工作,通常通过Southern blot杂交或聚合酶链反应(PCR)进行。我们在此描述了一种基于实时PCR和SYBR(R)Green I染料的快速,简单的基因型鉴定试验,无需使用荧光引物。野生型和目标等位基因之间的区别基于PCR设计,该设计导致每种产品的解链温度不同。基因型的鉴定在扩增后立即可见,不需要PCR后操作,从而降低了成本和时间。因此,尽管实时PCR扩增提高了灵敏度,但扩增后反应管永不打开的事实,降低了污染的风险并消除了错误,这在重复处理同一只小鼠系的数十个样品时很常见。我们提供的协议已在Math1基因敲除小鼠上进行了测试,但是通用的,可用于任何基因敲除生产线和实时热循环仪,而无需任何进一步的修改,附件或特殊试剂。

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